Search results for "paroxysmal dyskinesia"

The MalaCard for "paroxysmal dyskinesia" has been retired.
Searching MalaCards for entries containing "paroxysmal dyskinesia"

262 hits were found for 'paroxysmal dyskinesia'

# Family MCID Name MIFTS Score
1
FML185 Familial Paroxysmal Kinesigenic Dyskinesia 20 7.884
2
c FML186 Familial Paroxysmal Nonkinesigenic Dyskinesia 17 6.264
3
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 5.798
4
GNR006 Generalized Epilepsy and Paroxysmal Dyskinesia 19 5.790
5
P PRX004 Paroxysmal Nonkinesigenic Dyskinesia 31 5.234
6
P EPS030 Episodic Kinesigenic Dyskinesia 1 27 4.191
7
c PRX024 Paroxysmal Nonkinesigenic Dyskinesia 2 10 4.078
8
GLT019 Glut1 Deficiency Syndrome 2 32 3.608
9
PRX022 Paroxysmal Choreoathetosis 26 3.083
10
PRX086 Paroxysmal Exertion-Induced Dyskinesia 11 2.968
11
P PRM011 Primary Ciliary Dyskinesia 57 0.437
12
P DYS154 Dystonia 65 0.233
13
MVM001 Movement Disease 49 0.221
14
P EPL164 Epilepsy 66 0.188
15
DRG016 Drug Induced Dyskinesia 23 0.181
16
ALR002 Al-Raqad Syndrome 36 0.167
17
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.162
18
P PRK057 Parkinson Disease, Late-Onset 70 0.145
19
P HRT032 Heart Disease 75 0.142
20
BSL008 Basal Ganglia Disease 40 0.142
21
MYL009 Myelodysplastic Syndrome 73 0.136
22
HPT074 Hepatic Adenoma, Somatic 50 0.136
23
HNM002 Hinman Syndrome 25 0.134
24
P HML002 Hemolytic Anemia 62 0.134
25
VND001 Vein Disease 47 0.132
26
HDC001 Headache 54 0.127
27
c CNT035 Central Nervous System Disease 60 0.125
28
P NRV007 Nervous System Disease 71 0.124
29
AND005 Androgen Insensitivity Syndrome, Mild 16 0.117
30
c CRN175 Coronary Heart Disease 4 19 0.111
31
P ATX004 Ataxia 53 0.109
32
CRB009 Cerebritis 39 0.106
33
P ENC018 Encephalopathy 59 0.106
34
ADC005 Adcy5-Related Dyskinesia 10 0.104
35
c CRN214 Coronary Heart Disease 5 22 0.101
36
SLP005 Sleep Disorder 53 0.097
37
c PND001 Pain Disorder 54 0.096
38
P CRN178 Coronary Heart Disease 6 21 0.096
39
NRN002 Neuronitis 41 0.095
40
PRD011 Proud Syndrome 42 0.094
41
INN002 Inner Ear Disease 49 0.092
42
EXF001 Exfoliation Syndrome 57 0.091
43
P PLN008 Peeling Skin Syndrome 45 0.091
44
CSY001 C Syndrome 50 0.089
45
ATN002 Autonomic Nervous System Disease 48 0.089
46
c PLN018 Peeling Skin Syndrome 2 40 0.088
47
P TRM003 Tremor 54 0.084
48
WLF001 Wolff-Parkinson-White Syndrome 56 0.084
49
ATR060 Atrial Standstill, Digenic 51 0.084
50
CNT017 Central Nervous System Origin Vertigo 24 0.083
51
RTN023 Retinitis 50 0.082
52
VST004 Vestibular Disease 44 0.081
53
ADT003 Auditory System Disease 40 0.081
54
CHL071 Child Syndrome 58 0.080
55
KDS001 Kid Syndrome 53 0.080
56
STR067 Stroke, Ischemic 75 0.079
57
ISC004 Ischemia 61 0.079
58
DSS008 Disease of Mental Health 52 0.076
59
DYS140 Dyskinesia, Familial, with Facial Myokymia 23 0.076
60
P PSD015 Pseudohypoparathyroidism 46 0.075
61
PHY002 Physical Disorder 43 0.074
62
HYP056 Hypoglycemia 61 0.073
63
P HMP006 Hemiplegic Migraine 45 0.073
64
MTH009 Mouth Disease 61 0.073
65
P SZR006 Seizure Disorder 56 0.071
66
INS001 Insulinoma 61 0.070
67
c CHR096 Chronic Pulmonary Heart Disease 40 0.070
68
P CRD011 Cardiomyopathy 68 0.069
69
c EPS013 Episodic Kinesigenic Dyskinesia 2 9 0.069
70
P HPT021 Hepatitis 69 0.068
71
CRB039 Cerebrovascular Disease 63 0.068
72
c PLN017 Peeling Skin Syndrome 1 34 0.067
73
P PNM007 Pneumonia 68 0.067
74
MYC033 Myoclonus 42 0.067
75
WST001 West Syndrome 57 0.067
76
P GNR027 Generalized Peeling Skin Syndrome 19 0.065
77
SPS057 Spasticity 42 0.065
78
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 60 0.064
79
P CRB042 Cerebellar Ataxia 63 0.063
80
P FNC043 Fanconi Anemia, Complementation Group E 55 0.063
81
P CRV039 Cervicitis 45 0.063
82
c PLN021 Peeling Skin Syndrome 3 29 0.063
83
ATN005 Autonomic Dysfunction 49 0.063
84
RSP006 Respiratory System Disease 58 0.062
85
P INT063 Intellectual Disability 49 0.062
86
NSD001 Nose Disease 48 0.062
87
END072 Endotheliitis 42 0.061
88
ATH004 Athetosis 26 0.061
89
SYN036 Syncope 47 0.061
90
c VNT029 Ventricular Tachycardia, Catecholaminergic Polymorphic, 4 41 0.061
91
P HYP086 Hypothyroidism 64 0.058
92
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.058
93
CHR073 Choreatic Disease 37 0.058
94
PRX087 Paroxysomal Nonkinesigenic Dyskinesia 3 0.058
95
DDN006 Duodenitis 42 0.058
96
P SHR029 Short Syndrome 58 0.058
97
ACR041 Acromelic Frontonasal Dysostosis 45 0.058
98
P HYP265 Hypotonia 38 0.058
99
P HYP024 Hypoparathyroidism 53 0.058
100
P MGR003 Migraine with Aura 52 0.058
101
SPN033 Spontaneous Ocular Nystagmus 37 0.058
102
c DYS119 Dystonia 9 36 0.058
103
P MYP004 Myopathy 67 0.057
104
WLL006 Wells Syndrome 59 0.057
105
GDS001 Good Syndrome 44 0.057
106
c BNG023 Benign Familial Infantile Epilepsy 39 0.057
107
P AST005 Asthma 82 0.055
108
CHL067 Cholecystitis 57 0.055
109
P PNT019 Pontocerebellar Hypoplasia 38 0.055
110
P MNN013 Meningitis 67 0.054
111
P EPS003 Episodic Ataxia 57 0.054
112
FSC004 Fasciitis 48 0.054
113
P ENC004 Encephalitis 63 0.053
114
BRT030 Birth Defects 43 0.053
115
PCK002 Pick Disease 68 0.053
116
MSC004 Muscle Tissue Disease 34 0.053
117
P ESP024 Esophagitis 61 0.051
118
PLS006 Plasmodium Vivax Malaria 53 0.050
119
BRN080 Brain Ischemia 41 0.050
120
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.050
121
PYR013 Pyruvate Kinase Deficiency 58 0.048
122
P MSC033 Muscle Disorders 52 0.048
123
CLC006 Calcinosis 50 0.048
124
WTH001 Withdrawal Disorder 37 0.048
125
ADP007 Adie Pupil 34 0.048
126
P BPL003 Bipolar Disorder 62 0.046
127
MYL001 Myelitis 51 0.046
128
c PSD066 Pseudohypoparathyroidism, Type Ib 51 0.046
129
P GNR032 Generalized Dystonia 45 0.046
130
P BLP003 Blepharospasm 43 0.046
131
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.046
132
SCK003 Sickle Cell Anemia 71 0.046
133
P THL005 Thalassemia 64 0.046
134
CHR066 Chronic Fatigue Syndrome 64 0.046
135
P ALX003 Alexander Disease 63 0.046
136
HMG005 Hemoglobinopathy 52 0.046
137
BSL009 Basal Ganglia Calcification 43 0.046
138
LKC003 Leukocyte Disease 43 0.046
139
SPS019 Spastic Paraparesis 41 0.046
140
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.046
141
HMD003 Hemidystonia 26 0.046
142
PSY012 Psychogenic Movement 21 0.046
143
P MDL005 Medulloblastoma 77 0.041
144
CNS004 Constipation 57 0.041
145
DYS073 Dysphagia 48 0.041
146
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.041
147
CNT025 Central Pontine Myelinolysis 41 0.041
148
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.041
149
NSY001 N Syndrome 36 0.041
150
FCL011 Facial Nerve Disease 36 0.041
151
c AST037 Asthma 1 29 0.041
152
GNC005 Geniculate Ganglionitis 27 0.041
153
OST017 Osteomyelitis 61 0.040
154
STT001 Status Epilepticus 59 0.040
155
TRN015 Transient Cerebral Ischemia 56 0.040
156
VSC003 Visceral Leishmaniasis 56 0.040
157
P THY032 Thyroiditis 54 0.040
158
PMS001 Poems Syndrome 52 0.040
159
P BLD051 Blood Coagulation Disease 42 0.040
160
WBR001 Weber Syndrome 41 0.040
161
ADJ001 Adjustment Disorder 38 0.040
162
OCL011 Ocular Motility Disease 37 0.040
163
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.040
164
c SZR016 Seizures, Benign Familial Infantile, 2 22 0.040
165
c DLT002 Dilated Cardiomyopathy 76 0.034
166
WLS001 Wilson Disease 72 0.034
167
P LYN001 Lynch Syndrome 69 0.034
168
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.034
169
LSH001 Leishmaniasis 66 0.034
170
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.034
171
PRT037 Pertussis 64 0.034
172
CYS013 Cystinuria 63 0.034
173
P PRD006 Prader-Willi Syndrome 62 0.034
174
CRD119 Cardiac Arrest 61 0.034
175
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.034
176
P GRV001 Graves' Disease 59 0.034
177
INT066 Interstitial Lung Disease 59 0.034
178
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.034
179
P CTS001 Cutis Laxa 58 0.034
180
P MTR004 Maturity-Onset Diabetes of the Young 58 0.034
181
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.034
182
ABL002 Ablepharon-Macrostomia Syndrome 57 0.034
183
P INT143 Interstitial Cystitis 57 0.034
184
HYP266 Hypoxia 56 0.034
185
P OVR049 Ovarian Disease 56 0.034
186
NWC001 Newcastle Disease 54 0.034
187
PLN006 Poland Syndrome 54 0.034
188
THL016 Thalassemias, Alpha- 53 0.034
189
P NNT009 Neonatal Diabetes Mellitus 52 0.034
190
QDR001 Quadriplegia 52 0.034
191
ALL026 Allergic Hypersensitivity Disease 52 0.034
192
PRC013 Pericarditis 51 0.034
193
APP015 Apparent Mineralocorticoid Excess 51 0.034
194
HYP005 Hypokalemia 51 0.034
195
SPN051 Spondylitis 51 0.034
196
RDC002 Radiculopathy 50 0.034
197
SPR099 Supravalvar Aortic Stenosis 49 0.034
198
c CNG464 Congenital Myopathy 49 0.034
199
THL018 Thalassemia Major 48 0.034
200
RTN020 Retinal Vascular Disease 48 0.034
201
RNP001 Renpenning Syndrome 47 0.034
202
P MYT023 Myotonia Congenita 47 0.034
203
P PTT014 Pitt-Hopkins Syndrome 47 0.034
204
PLY012 Polyhydramnios 47 0.034
205
HYP043 Hyperandrogenism 47 0.034
206
IDP064 Idiopathic Neutropenia 45 0.034
207
CRB090 Cerebral Hypoxia 45 0.034
208
RNL097 Renal Artery Disease 43 0.034
209
LKM006 Leukomalacia 43 0.034
210
PRT003 Partington Syndrome 43 0.034
211
BHR001 Behr Syndrome 42 0.034
212
c RTN055 Retinitis Pigmentosa 26 41 0.034
213
IMP006 Impulse Control Disorder 40 0.034
214
CRN031 Cranial Nerve Disease 40 0.034
215
HYD038 Hydrops Fetalis, Nonimmune 40 0.034
216
SPN369 Spinal Disease 39 0.034
217
HYP026 Hypoglycemic Coma 39 0.034
218
HMG025 Hemoglobin H Disease, Nondeletional 39 0.034
219
HNZ001 Heinz Body Anemia 39 0.034
220
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 38 0.034
221
BLD054 Blood Protein Disease 37 0.034
222
ALP093 Alpha-Thalassemia/mental Retardation Syndrome, Chromosome 16-Related 37 0.034
223
c MCR120 Microvascular Complications of Diabetes 7 37 0.034
224
c DBT049 Diabetes Mellitus, Insulin-Dependent, 13 37 0.034
225
c DBT048 Diabetes Mellitus, Insulin-Dependent, 11 36 0.034
226
KLN009 Kleine-Levin Hibernation Syndrome 36 0.034
227
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 36 0.034
228
MYT011 Myotonia 36 0.034
229
c DBT058 Diabetes Mellitus, Insulin-Dependent, 7 35 0.034
230
P EXT032 Extraosseous Osteosarcoma 35 0.034
231
BCK003 Background Diabetic Retinopathy 34 0.034
232
RBS002 Rubeosis Iridis 34 0.034
233
c DBT054 Diabetes Mellitus, Insulin-Dependent, 24 34 0.034
234
c DBT038 Diabetes Mellitus, Insulin-Dependent, 5 34 0.034
235
IMM039 Immune Hydrops Fetalis 33 0.034
236
P LTT001 Lattice Corneal Dystrophy 33 0.034
237
HYP110 Hyperproinsulinemia 32 0.034
238
c CTS019 Cutis Laxa, Ad 31 0.034
239
VSL002 Visual Epilepsy 31 0.034
240
BRN008 Brain Compression 30 0.034
241
P PRD037 Periodontal Ehlers-Danlos Syndrome 30 0.034
242
PRN032 Paraneoplastic Cerebellar Degeneration 30 0.034
243
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.034
244
ALP094 Alpha Thalassemia-Intellectual Disability Syndrome Type 1 29 0.034
245
MTH064 Methemoglobinemia, Beta-Globin Type 29 0.034
246
c AST039 Asthma 2 28 0.034
247
MDD015 Mid-Dermal Elastolysis 28 0.034
248
NRG003 Neurogenic Arthropathy 28 0.034
249
c CTS008 Cutis Laxa, Autosomal Dominant 28 0.034
250
P PRD017 Periodic Paralyses 27 0.034
251
IMM002 Immature Cataract 27 0.034
252
c ACQ027 Acquired Cutis Laxa 27 0.034
253
SHP003 Shapiro Syndrome 26 0.034
254
BRC002 Brachial Plexus Neuritis 26 0.034
255
PRL014 Paralytic Squint 25 0.034
256
PRN033 Paraneoplastic Neurologic Disorders 25 0.034
257
c ERL003 Early Onset Absence Epilepsy 25 0.034
258
ATS203 Autosomal Dominant Non-Syndromic Intellectual Disability 23 0.034
259
MND006 Mondor Disease 21 0.034
260
c CRN174 Coronary Heart Disease 2 20 0.034
261
c FBL003 Fbln5-Related Cutis Laxa 16 0.034
262
c BNG076 Benign Exophthalmos Syndrome 15 0.034